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Clinical significance of kallikrein 5 as a novel prognostic biomarker in gastric adenocarcinoma

BACKGROUNDS: Gastric cancer is one of the most common cancers with unsatisfied prognosis. It is challenging to predict gastric cancer prognosis due to its highly heterogeneous nature. Kallikrein 5 (KLK5) belongs to the family of kallikreins, which plays a crucial role in serine proteolysis and exert...

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Autores principales: Abuduhadeer, Xiaokaiti, Xu, Xincai, Aihesan, Kamali, Yilihamu, Maimaiti, Zhao, Yanjun, Zhang, Wenbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529136/
https://www.ncbi.nlm.nih.gov/pubmed/34510543
http://dx.doi.org/10.1002/jcla.23958
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author Abuduhadeer, Xiaokaiti
Xu, Xincai
Aihesan, Kamali
Yilihamu, Maimaiti
Zhao, Yanjun
Zhang, Wenbin
author_facet Abuduhadeer, Xiaokaiti
Xu, Xincai
Aihesan, Kamali
Yilihamu, Maimaiti
Zhao, Yanjun
Zhang, Wenbin
author_sort Abuduhadeer, Xiaokaiti
collection PubMed
description BACKGROUNDS: Gastric cancer is one of the most common cancers with unsatisfied prognosis. It is challenging to predict gastric cancer prognosis due to its highly heterogeneous nature. Kallikrein 5 (KLK5) belongs to the family of kallikreins, which plays a crucial role in serine proteolysis and exerts diverse physiological functions. The role of KLK5 in human gastric adenocarcinoma (GAC) has not been elucidated. In the present study, we aimed to examine the expression level of KLK5 and dissect whether the KLK5 expression was associated with GAC prognosis. PATIENTS AND METHODS: Clinicopathological analyses were performed in a retrospective GAC patient cohort (n = 138). The expression of KLK5 was tested by quantitative RT‐PCR and immunohistochemistry staining. The prognostic role of KLK5 in GAC was assessed by univariate and multivariate analyses. The effects of KLK5 on cell proliferation, migration, and invasion were examined through cellular experiments. RESULTS: The data showed that KLK5 expression was elevated in GAC tissues compared with normal stomach tissues. Protein expression of KLK5 was positively correlated with tumor invasion depth and lymph node metastasis. Patients with higher KLK5 expression had poorer overall survival. KLK5 was identified to be an independent risk factor according to multivariate analysis. Using human GAC cell lines, we found that KLK5 can promote tumor cell migration and invasion. CONCLUSIONS: Our study demonstrated that higher expression of KLK5 was significantly correlated with a poorer prognosis of GAC patients, implying the potential of KLK5 as a novel prognostic biomarker in GAC.
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spelling pubmed-85291362021-10-27 Clinical significance of kallikrein 5 as a novel prognostic biomarker in gastric adenocarcinoma Abuduhadeer, Xiaokaiti Xu, Xincai Aihesan, Kamali Yilihamu, Maimaiti Zhao, Yanjun Zhang, Wenbin J Clin Lab Anal Research Articles BACKGROUNDS: Gastric cancer is one of the most common cancers with unsatisfied prognosis. It is challenging to predict gastric cancer prognosis due to its highly heterogeneous nature. Kallikrein 5 (KLK5) belongs to the family of kallikreins, which plays a crucial role in serine proteolysis and exerts diverse physiological functions. The role of KLK5 in human gastric adenocarcinoma (GAC) has not been elucidated. In the present study, we aimed to examine the expression level of KLK5 and dissect whether the KLK5 expression was associated with GAC prognosis. PATIENTS AND METHODS: Clinicopathological analyses were performed in a retrospective GAC patient cohort (n = 138). The expression of KLK5 was tested by quantitative RT‐PCR and immunohistochemistry staining. The prognostic role of KLK5 in GAC was assessed by univariate and multivariate analyses. The effects of KLK5 on cell proliferation, migration, and invasion were examined through cellular experiments. RESULTS: The data showed that KLK5 expression was elevated in GAC tissues compared with normal stomach tissues. Protein expression of KLK5 was positively correlated with tumor invasion depth and lymph node metastasis. Patients with higher KLK5 expression had poorer overall survival. KLK5 was identified to be an independent risk factor according to multivariate analysis. Using human GAC cell lines, we found that KLK5 can promote tumor cell migration and invasion. CONCLUSIONS: Our study demonstrated that higher expression of KLK5 was significantly correlated with a poorer prognosis of GAC patients, implying the potential of KLK5 as a novel prognostic biomarker in GAC. John Wiley and Sons Inc. 2021-09-12 /pmc/articles/PMC8529136/ /pubmed/34510543 http://dx.doi.org/10.1002/jcla.23958 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Abuduhadeer, Xiaokaiti
Xu, Xincai
Aihesan, Kamali
Yilihamu, Maimaiti
Zhao, Yanjun
Zhang, Wenbin
Clinical significance of kallikrein 5 as a novel prognostic biomarker in gastric adenocarcinoma
title Clinical significance of kallikrein 5 as a novel prognostic biomarker in gastric adenocarcinoma
title_full Clinical significance of kallikrein 5 as a novel prognostic biomarker in gastric adenocarcinoma
title_fullStr Clinical significance of kallikrein 5 as a novel prognostic biomarker in gastric adenocarcinoma
title_full_unstemmed Clinical significance of kallikrein 5 as a novel prognostic biomarker in gastric adenocarcinoma
title_short Clinical significance of kallikrein 5 as a novel prognostic biomarker in gastric adenocarcinoma
title_sort clinical significance of kallikrein 5 as a novel prognostic biomarker in gastric adenocarcinoma
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529136/
https://www.ncbi.nlm.nih.gov/pubmed/34510543
http://dx.doi.org/10.1002/jcla.23958
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